Canonical Allele Identifier: CA446310094
Gene: FBN2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.127670968G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.128335276G>A , CM000667.2:g.128335276G>A GRCh38
NC_000005.9:g.127670968G>A , CM000667.1:g.127670968G>A GRCh37
NC_000005.8:g.127698867G>A NCBI36
NG_008750.1:g.207768C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703783.1:n.651C>T
ENST00000703785.1:n.732C>T
ENST00000262464.9:c.3867C>T MANE Select ENSP00000262464.4:p.Asn1289=
ENST00000262464.8:c.3867C>T ENSP00000262464.4:p.Asn1289=
ENST00000507835.5:c.417C>T ENSP00000426839.1:p.Asn139=
ENST00000508053.5:c.3867C>T ENSP00000424571.1:p.Asn1289=
ENST00000508989.5:c.3768C>T ENSP00000425596.1:p.Asn1256=
ENST00000619499.4:c.3864C>T ENSP00000482132.1:p.Asn1288=
NM_001999.3:c.3867C>T NP_001990.2:p.Asn1289=
XM_017009228.2:c.3714C>T XP_016864717.1:p.Asn1238=
NM_001999.4:c.3867C>T MANE Select NP_001990.2:p.Asn1289=